Insight into membrane selectivity of linear and branched polyethylenimines and their potential as biocides for advanced wound dressings

被引:36
作者
Fox, Stephen John [1 ]
Fazil, Mobashar Hussain Urf Turabe [2 ]
Dhand, Chetna [3 ]
Venkatesh, Mayandi [3 ]
Goh, Eunice Tze Leng [3 ]
Harini, Sriram [3 ]
Eugene, Christo [3 ]
Lim, Rayne Rui [4 ]
Ramakrishna, Seeram [5 ]
Chaurasia, Shyam Sunder [4 ]
Beuerman, Roger W. [3 ,6 ]
Verma, Chandra Shekhar [1 ,7 ,8 ]
Verma, Navin Kumar [2 ]
Loh, Xian Jun [9 ]
Lakshminarayanan, Rajamani [3 ,6 ]
机构
[1] ASTAR, Bioinformat Inst, Singapore 138671, Singapore
[2] Nanyang Technol Univ, Lee Kong Chian Sch Med, Expt Med Bldg, Singapore 636921, Singapore
[3] Singapore Eye Res Inst, Antiinfect Res Grp, Singapore 169856, Singapore
[4] Univ Missouri, Dept Vet Med & Surg, Ocular Immunol & Angiogenesis Lab, Columbia, MO 65211 USA
[5] Natl Univ Singapore, Dept Mech Engn, Singapore 117576, Singapore
[6] Duke NUS Grad Med Sch, SRP Neurosci & Behav Disorders, Singapore 169857, Singapore
[7] Nanyang Technol Univ, Sch Biol Sci, 60 Nanyang Dr, Singapore 637551, Singapore
[8] Natl Univ Singapore, Dept Biol Sci, 14 Sci Dr 4, Singapore 117543, Singapore
[9] ASTAR, Inst Mat Res & Engn, 2 Fusionopolis Way,Innovis 08-03, Singapore 138634, Singapore
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Molecular dynamics; Membrane selectivity; Polyethylenimine; Electrospinning; Contact-mediated antibacterials; BACTERIAL-MEMBRANE; POLYETHYLENEIMINE NANOPARTICLES; ANTIBACTERIAL APPLICATIONS; STAPHYLOCOCCUS-AUREUS; GENE DELIVERY; FORCE-FIELD; SOFT-TISSUE; THIN-FILMS; INFECTIONS; BIOCOMPATIBILITY;
D O I
10.1016/j.actbio.2016.04.015
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
We report here structure-property relationship between linear and branched polyethylene imines by examining their antimicrobial activities against wide range of pathogens. Both the polymers target the cytoplasmic membrane of bacteria and yeasts, eliciting rapid microbicidal properties. Using multiscale molecular dynamic simulations, we showed that, in both fully or partially protonated forms LPEI discriminates between mammalian and bacterial model membranes whereas BPEI lacks selectivity for both the model membranes. Simulation results suggest that LPEI forms weak complex with the zwitterionic lipids whereas the side chain amino groups of BPEI sequester the zwitterionic lipids by forming tight complex. Consistent with these observations, label-free cell impedance measurements, cell viability assays and high content analysis indicate that BPEI is cytotoxic to human epithelial and fibroblasts cells. Crosslinking of BPEI onto electrospun gelatin mats attenuate the cytotoxicity for fibroblasts while retaining the antimicrobial activity against Gram-positive and yeasts strains. PEI crosslinked gelatin mats elicit bactericidal activity by contact-mediated killing and durable to leaching for 7 days. The potent antimicrobial activity combined with enhanced selectivity of the crosslinked ES gelatin mats would expand the arsenel of biocides in the management of superficial skin infections. The contact-mediated microbicidal properties may avert antimicrobial resistance and expand the diversity of applications to prevent microbial contamination. Statement of Significance Current commercially available advanced wound dressings are either impregnated with metallic silver or silver salts which have side effects or may not avert antimicrobial resistance. In this article, we have used multidisciplinary approach comprising of computational, chemical and biological methods to understand the antimicrobial properties and biocompatibility of linear (LPEI) and branched (BPEI) polyethylenimines. We then applied this knowledge to develop dual purpose wound dressings containing these polymers, which encourages healing while maintain antimicrobial activity. In addition, the approach can be expanded to rationalize the antimicrobial vs. cytotoxicity of other cationic polymers and the method of crosslinking would enhance their potentials as biocides for advanced materials. (c) 2016 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:155 / 164
页数:10
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